CFTR-NGS variants catalogue
Variant hg19:chr7:117258532T/TCACA
Name | NM_000492.4:c.3468+3790_3468+3793dupCACA |
Protein name | NP_000483.3:p.(?) |
Genomic name (hg19) | chr7:g.117258557_117258560dup UCSC |
#Exon/intron | intron 21 |
Type in CFTR-NGS catalogue | microsatellite |
Class in CFTR-France | not reported |
WT sequence | ACACACACACACACACACACACACA ---- AAGAAAATAAACCATCTCTTGATGA |
Mutant sequence | ACACACACACACACACACACACACA CACA AAGAAAATAAACCATCTCTTGATGA |
MAF (GnomAD) | 5.25e-03 |
Splicing prediction (SpliceAI) | - |
![]() Not found | ![]() Not found | dbSNP no rs | ![]() Not found | ![]() |
Sanger (present/not present/not verified) |
Minigene (effect/no effect/not performed) |
not verified | not performed |
No patient found in CFTR-France |
TOTAL NUMBER OF INDIVIDUALS | 1 |
---|---|
CF | 1 |
ID | Phenotype | Laboratory | Experiment | Variant status | Variant filter | Quality score | Depth of coverage |
---|---|---|---|---|---|---|---|
9078 | CF | Montpellier | 160218_varilh | heterozygous | PASS | 1520 | 134 |